PMID- 22015915 OWN - NLM STAT- MEDLINE DCOM- 20130802 LR - 20211203 IS - 1090-2430 (Electronic) IS - 0014-4886 (Print) IS - 0014-4886 (Linking) VI - 244 DP - 2013 Jun TI - Mammalian target of rapamycin (mTOR) activation in focal cortical dysplasia and related focal cortical malformations. PG - 22-6 LID - S0014-4886(11)00360-8 [pii] LID - 10.1016/j.expneurol.2011.10.002 [doi] AB - Focal cortical dysplasia (FCD) and other localized malformations of cortical development represent common causes of intractable pediatric epilepsy. Insights into the cellular and molecular pathogenesis of focal cortical malformations may reveal information about associated mechanisms of epileptogenesis and suggest new therapies for seizures caused by these developmental lesions. In animal models and human studies of FCD and the related disease of Tuberous Sclerosis Complex (TSC), the mammalian target of rapamycin (mTOR) pathway has been implicated in mediating cellular and molecular changes leading to the formation of the cortical malformations and the expression of epilepsy. The use of mTOR inhibitors may represent a rational therapeutic strategy for treating or even preventing epilepsy due to FCD and TSC. CI - Copyright (c) 2011 Elsevier Inc. All rights reserved. FAU - Wong, Michael AU - Wong M AD - Department of Neurology and the Hope Center for Neurological Disorders, Washington University School of Medicine, St. Louis, MO 63110, USA. wong_m@wustl.edu LA - eng GR - R01 NS056872/NS/NINDS NIH HHS/United States GR - R01 NS056872-06/NS/NINDS NIH HHS/United States PT - Journal Article PT - Review DEP - 20111008 PL - United States TA - Exp Neurol JT - Experimental neurology JID - 0370712 RN - EC 2.7.1.1 (MTOR protein, human) RN - EC 2.7.11.1 (TOR Serine-Threonine Kinases) SB - IM MH - Animals MH - Humans MH - Malformations of Cortical Development/*metabolism/pathology MH - Signal Transduction/*physiology MH - TOR Serine-Threonine Kinases/*metabolism MH - Tuberous Sclerosis/*metabolism/pathology PMC - PMC3265661 MID - NIHMS331571 EDAT- 2011/10/22 06:00 MHDA- 2013/08/03 06:00 PMCR- 2014/06/01 CRDT- 2011/10/22 06:00 PHST- 2011/05/19 00:00 [received] PHST- 2011/10/03 00:00 [accepted] PHST- 2011/10/22 06:00 [entrez] PHST- 2011/10/22 06:00 [pubmed] PHST- 2013/08/03 06:00 [medline] PHST- 2014/06/01 00:00 [pmc-release] AID - S0014-4886(11)00360-8 [pii] AID - 10.1016/j.expneurol.2011.10.002 [doi] PST - ppublish SO - Exp Neurol. 2013 Jun;244:22-6. doi: 10.1016/j.expneurol.2011.10.002. Epub 2011 Oct 8.